FoodApr 29, 2026
Marquez Brothers International EL MEXICANO horchata casera Instant Horchata Drink NET WT recall — FDA H-0673-2026
Undeclared milk.
Class IIFDA: OngoingMarquez Brothers International, Inc.
April 2026 recalls — page 4
These records include useful source details for the selected month.
FoodApr 29, 2026
Marquez Brothers International EL MEXICANO agua fresca de horchata Instant Horchata Drink recall — FDA H-0674-2026
Undeclared milk.
Class IIFDA: OngoingMarquez Brothers International, Inc.
FoodApr 29, 2026
Unistel Industries SALUTE SEASONINGS recall — FDA H-0666-2026
Product may be contaminated with Salmonella.
Class IFDA: TerminatedUnistel Industries Inc.
FoodApr 29, 2026
Marquez Brothers International Bulk Horchata Powder 3951 recall — FDA H-0672-2026
Undeclared milk.
Class IIFDA: OngoingMarquez Brothers International, Inc.
FoodApr 29, 2026
Ethnic Foods Bombay Kitchen brand Punjabi Mix recall — FDA H-0670-2026
Product(s) contain undeclared colors, FD&C Yellow #6 and FD&C Red #40
Class IIFDA: TerminatedEthnic Foods Inc
FoodApr 29, 2026
Costco Wholesale Kirkland Signature Traditional Madeleines 12 Count/net wt recall — FDA H-0682-2026
Undeclared hazelnut and soy lecithin.
Class IFDA: TerminatedCostco Wholesale Corporation
FoodApr 29, 2026
Ethnic Foods Bombay Kitchen brand Tikka Sev recall — FDA H-0669-2026
Product(s) contain undeclared colors, FD&C Yellow #6 and FD&C Red #40
Class IIFDA: TerminatedEthnic Foods Inc
DrugApr 29, 2026
Pantoprazole Sodium, Delayed-Release Tablets, USP, 40 mg, 1000-count bottle recall — FDA D-0484-2026
Discoloration: Firm received five (5) complaints stating that, "Tablets discolored darker than normal and have lighter-colored spots."
Class IIFDA: OngoingHetero Labs Limited (Unit V)
DrugApr 29, 2026
Claravis recall — FDA D-0521-2026
Failed Impurities/Degradation Specifications: Out of specification for specific impurity Tretinoin
Class IIFDA: OngoingTeva Pharmaceuticals USA, Inc
DrugApr 29, 2026
MONSELS SOLUTION Premier, Monsel's, Ferric Subsulfate Solution, 8 mL bottles recall — FDA D-0490-2026
Labeling: Incorrect or Missing Lot and/or Exp Date:The expiration date has an extra digit and is printed as 2709114 instead of the correct 270914 (2027-09-14). It is important to note that…
Class IIIFDA: OngoingPremier Dental Products Co
DrugApr 29, 2026
OMEGA-3-ACID ETHYL ESTERS Omega-3-Acid, Ethyl Esters, Capsules, USP, 1 gram, 50 capsules recall — FDA D-0493-2026
Failed Capsule Specifications: Out of specification results obtained during routine stability testing for Loss on Drying of Capsule Shells.
Class IIFDA: OngoingThe Harvard Drug Group LLC
Medical DeviceApr 22, 2026
B Braun Medical B. Braun Hemodialysis Bloodlines, STREAMLINE BLOODLINE SET FOR DIALOG recall — FDA Z-1799-2026
Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
Class IFDA: OngoingB Braun Medical Inc
Medical DeviceApr 22, 2026
B Braun Medical B. Braun Hemodialysis Bloodlines, LOW VOL, NO CHAMBER 2.6MM PUMP SEGMENT recall — FDA Z-1802-2026
Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
Class IFDA: OngoingB Braun Medical Inc
Medical DeviceApr 22, 2026
B Braun Medical B Braun Hemodialysis Bloodlines, LOW VOL, NO CHAMBER 4.8MM PUMP SEGMENT recall — FDA Z-1803-2026
Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
Class IFDA: OngoingB Braun Medical Inc
Medical DeviceApr 22, 2026
LinkBio CORE Workstation, a component of the CORE Shoulder System recall — FDA Z-1810-2026
The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen.
Class IIFDA: OngoingLinkbio Corp.
Medical DeviceApr 22, 2026
B Braun Medical B. Braun Hemodialysis Bloodlines, STREAMLINE FRESENIUS FOR DAVITA recall — FDA Z-1800-2026
Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
Class IFDA: OngoingB Braun Medical Inc
Medical DeviceApr 22, 2026
B Braun Medical B. Braun Hemodialysis Bloodlines, STREAMLINE BLOODLINE SET FOR DIALOG DR recall — FDA Z-1798-2026
Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
Class IFDA: OngoingB Braun Medical Inc
Medical DeviceApr 22, 2026
Siemens Medical Solutions USA ARTIS Pheno VE30A and VE40A, Model 10849000 recall — FDA Z-1814-2026
During 3D acquisitions, lighter and darker patient images may be captured, which may result in less accurate 3D reconstruction. The variation of brightness is a result of a constant…
Class IIFDA: OngoingSiemens Medical Solutions USA, Inc
Medical DeviceApr 22, 2026
Philips Spectral CT on Rails recall — FDA Z-1825-2026
Philips has identified three software issues: 1. During a continuous CT (CCT) scan, there is the potential that the Gantry could remain at the current scan position after pressing Go. 2.…
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS
Medical DeviceApr 22, 2026
B Braun Medical B. Barun Hemodialysis Bloodlines, StreamLine Bloodline Long Version, FMC recall — FDA Z-1801-2026
Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
Class IFDA: OngoingB Braun Medical Inc
Medical DeviceApr 22, 2026
ELEGANCE 1 LEVEL CERVICAL PLATE, ELEGANCE 2 LEVEL CERVICAL PLATE, ELEGANCE 3 LEVEL CERVICAL recall — FDA Z-1821-2026
Due to a quality issue regarding the presence of burr on the finished cervical plate product.
Class IIFDA: OngoingClariance-SAS
Medical DeviceApr 22, 2026
Beta Bionics iLet Ace Pump Kit REF: BB1001 iLet Dosing Decision Software recall — FDA Z-1809-2026
it was found that in versions 1.3.7, 1.4.2, and 1.4.3, the Lock Screen and Limited Access Passcode Screen on the iLet graphical user interface (GUI) include certain icons displayed in the…
Class IIFDA: OngoingBeta Bionics, Inc.
Medical DeviceApr 22, 2026
Philips AneurysmFlow recall — FDA Z-1805-2026
Potential safety issue involving the Mean Aneurysm Flow Amplitude (MAFA) ratio of AneurysmFlow (Interventional Tool). Philips has determined that the MAFA ratio does not provide reliable…
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceApr 22, 2026
CELLEX Photopheresis Kit recall — FDA Z-1822-2026
Increased difficulty in installing the centrifuge bowl onto the centrifuge bowl holder. Improper installation may cause the centrifuge bowl to dislodge, resulting in a broken bowl during…
Class IIFDA: OngoingTHERAKOS DEVELOPMENT LIMITED
How to use this monthly recall archive
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.